Disease: Low density lipoprotein cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 6
rs821840
CETP
16 56959974 upstream gene variant A/G snv 4
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 6
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs17120434
PCSK7 ; TAGLN
11 117204969 3 prime UTR variant A/G;T snv 5.4E-02 3
rs2255141
GPAM
10 112174128 intron variant A/G;T snv 5
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10889348
DOCK7
1 62612551 intron variant A/T snv 0.32 4
rs17031710
ABCG8 ; LOC102725159
2 43843754 intron variant A/T snv 2.1E-02 4
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs5743316
TLR3
4 186082537 missense variant A/T snv 4.0E-05 3.5E-05 3
rs9912177
ITGB3
17 47285851 intron variant A/T snv 6.4E-03 3
rs150641967
HAPLN4
19 19259532 intron variant AGAC/-;AGACAGAC delins 4
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 6
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 5
rs12721235
AGTR1
3 148722587 intron variant C/A snv 1.7E-02 4
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs16940391
LIPC
15 58507449 intron variant C/A;G snv 3